Asymmetric Total Synthesis of (+)-Strychnine

Org Lett. 2019 Jan 4;21(1):252-255. doi: 10.1021/acs.orglett.8b03686. Epub 2018 Dec 18.

Abstract

A synthetic strategy for the catalytic asymmetric total synthesis of (+)-strychnine is disclosed. Key features of this synthesis include an organocatalytic enantioselective Michael addition to establish the chirality of the starting building block, a photoinduced radical cascade reaction to access the Corynanthe alkaloid intermediate, and a bioinspired cascade rearrangement to generate the core of the Strychnos alkaloids.

Publication types

  • Research Support, Non-U.S. Gov't